Paradox Inc
FDA inspection history in Saint Joseph, Missouri, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Saint Joseph, Missouri.
Cited most
Across all Paradox observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.58Maintenance1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Paradox file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Saint Joseph, Missouri
One Form 483 · 2024 · 4 observations
Latest: Form 483, Oct 11, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-11 | 483 Form 483 | Saint Joseph, Missouri | 4 | $99 |
Investigators on these documents
FEI number 1927976 · most recent document Oct 11, 2024
About Paradox Inc
How many FDA Form 483s has Paradox Inc received?
FDA Intel has 1 Form 483 on file for Paradox Inc; the most recent is dated Oct 11, 2024.
When was Paradox Inc last inspected by FDA?
The most recent FDA inspection document on file for Paradox Inc is a Form 483 dated Oct 11, 2024, for the site in Saint Joseph, Missouri.
What did FDA cite at Paradox Inc?
The regulations cited most in the observations on file for Paradox Inc are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.58 (Maintenance), 1 time.